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Quoted phrase not found in phrase index: "Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome"
Page 1
Familial pseudo-Wolff-Parkinson-White syndrome.
Sternick EB, Oliva A, Magalhães LP, Gerken LM, Hong K, Santana O, Brugada P, Brugada J, Brugada R. Sternick EB, et al. J Cardiovasc Electrophysiol. 2006 Jul;17(7):724-32. doi: 10.1111/j.1540-8167.2006.00485.x. J Cardiovasc Electrophysiol. 2006. PMID: 16836667
INTRODUCTION: PRKAG2 plays a role in regulating metabolic pathways, and mutations in this gene are associated with familial ventricular preexcitation, hypertrophic cardiomyopathy, and atrioventricular conduction disturbances. ...Three individuals died suddenl …
INTRODUCTION: PRKAG2 plays a role in regulating metabolic pathways, and mutations in this gene are associated with familial ventricul …
Mutation of the MYH7 gene in a child with hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome.
Bobkowski W, Sobieszczańska M, Turska-Kmieć A, Nowak A, Jagielski J, Gonerska M, Lebioda A, Siwińska A. Bobkowski W, et al. J Appl Genet. 2007;48(2):185-8. doi: 10.1007/BF03194677. J Appl Genet. 2007. PMID: 17495353
Familial hypertrophic cardiomyopathy (HCM) displays autosomal dominant inheritance with incomplete penetration of defective genes. Data concerning the familial occurrence of ventricular preexcitation, i.e. Wolff-Parkinson-White (WP …
Familial hypertrophic cardiomyopathy (HCM) displays autosomal dominant inheritance with incomplete penetration of defec …
Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3.
MacRae CA, Ghaisas N, Kass S, Donnelly S, Basson CT, Watkins HC, Anan R, Thierfelder LH, McGarry K, Rowland E, et al. MacRae CA, et al. J Clin Invest. 1995 Sep;96(3):1216-20. doi: 10.1172/JCI118154. J Clin Invest. 1995. PMID: 7657794 Free PMC article.
We have mapped a disease locus for Wolff-Parkinson-White syndrome (WPW) and familial hypertrophic cardiomyopathy (FHC) segregating in a large kindred to chromosome 7 band q3. Although WPW syndrome and FHC have been observ …
We have mapped a disease locus for Wolff-Parkinson-White syndrome (WPW) and familial hypertrophic …
Electrophysiologic characteristics of accessory atrioventricular connections in an inherited form of Wolff-Parkinson-White syndrome.
Mehdirad AA, Fatkin D, DiMarco JP, MacRae CA, Wase A, Seidman JG, Seidman CE, Benson DW. Mehdirad AA, et al. J Cardiovasc Electrophysiol. 1999 May;10(5):629-35. doi: 10.1111/j.1540-8167.1999.tb00239.x. J Cardiovasc Electrophysiol. 1999. PMID: 10355918
INTRODUCTION: A familial form of Wolff-Parkinson-White syndrome (WPW) occurs in association with hypertrophic cardiomyopathy and intraventricular conduction abnormalities. This syndrome, demonstrating autosomal dominant inhe …
INTRODUCTION: A familial form of Wolff-Parkinson-White syndrome (WPW) occurs in association with hyper …